Explain the selection of enantiomerically pure

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The selection of enantiomerically pure (1S)-[endo]-(-)-borneol in the upcoming experiment presents a great opportunity to review some stereochemistry basics. Let us look at these stereochemical relationships. In the spaces provide below draw the three compounds named. A. (1R)-(+)-camphor B. (1R)-[exo]-(-)-isoborneol C. (1R)-(+)-borneol

Reference no: EM13153218

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